Effect of dietary supplementation of Bacillus subtilis B10 on biochemical and molecular parameters in the serum and liver of high-fat diet-induced obese mice

• Published in: Journal of Zhejiang University. B. Science 2015-06, Vol.16 (6), p.487-495
• Main Authors: Lei, Kai, Li, Ya-li, Wang, Yang, Wen, Jing, Wu, Hong-zhao, Yu, Dong-you, Li, Wei-fen
• Format: Article
• Language: English
• Subjects: Administration, Oral; Animals; Bacillus subtilis - physiology; Biomedical and Life Sciences; Biomedicine; Dietary Fats; Energy Metabolism; Lipid Metabolism; Male; Mice; Mice, Inbred ICR; Obesity - diet therapy; Obesity - metabolism; Obesity - microbiology; Probiotics - administration & dosage; Reactive Oxygen Species - blood; Reactive Oxygen Species - metabolism; Treatment Outcome
• ISSN: 1673-1581; 1862-1783
• DOI: 10.1631/jzus.B1400342

While a high-fat diet (HFD) is assumed to be related to fat-mediated oxidative stress decreasing antioxidant enzyme activity, probiotics are believed to have positive effects on the regulation of HFD-induced obesity as well as lipid metabolism, energy homeostasis, and anti-oxidation. Because Bacillus subtilis B10 has beneficial effects on the abnormal lipid metabolism and the oxidative stress in HFD-induced obese mice, ICR mice were randomly assigned into an HFD group and the HFD was supplemented with 0.1% (w/w) Bacillus subtilis B10 (HFD+B10 group). Thereafter, 30-d treatments were run, and then hepatic lipid level and antioxidant status were measured. The expression of genes related to lipid metabolism and oxidative stress in the liver was determined by reverse-transcription quantitative polymerase chain reaction (RT-qPCR). We found that HFD-induced obese mice treated with B10 showed a decrease in weight gain, serum glucose activity as well as hepatic triglyceride (TG), glutamic oxaloacetic transaminase (GOT), and glutamic pyruvic transaminase (GPT) activities. In addition, the gene expressions of antioxidant genes, glutathione reductase ( GR ), xanthine oxidase (XO), heat-shock protein 90 (Hsp90), and lipid synthesis gene 3β-hydroxysteroid-Δ24 reductase ( DHCR24 ) in the HFD+B10 group were down-regulated, suggesting alleviation of oxidative stress, while the lipolysis gene 3-hydroxy-3-methylglutaryl-CoA synthase 2 ( HMGCS2 ), energy metabolism gene peroxisome proliferator-activated receptor α ( PPARα ) and the gene encoding tumor-suppressor protein p53 were up-regulated. The regulatory and positive effect of dietary supplementation of probiotic B10 suggests that it has a beneficial effect on the homeostasis of the lipid metabolism and on alleviating oxidative stress in HFD-induced obese mice.